JP2005510607A5 - - Google Patents

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JP2005510607A5
JP2005510607A5 JP2003547500A JP2003547500A JP2005510607A5 JP 2005510607 A5 JP2005510607 A5 JP 2005510607A5 JP 2003547500 A JP2003547500 A JP 2003547500A JP 2003547500 A JP2003547500 A JP 2003547500A JP 2005510607 A5 JP2005510607 A5 JP 2005510607A5
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Japan
Prior art keywords
group
independently
formula
aqueous
hydrogen
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Pending
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JP2003547500A
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Japanese (ja)
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JP2005510607A (en
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Priority claimed from US09/994,561 external-priority patent/US20030113555A1/en
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Publication of JP2005510607A publication Critical patent/JP2005510607A/en
Publication of JP2005510607A5 publication Critical patent/JP2005510607A5/ja
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Claims (5)

(a)式Iの、少なくとも1種類の自己乳化性フッ素化アルコキシシラン、
f 1−[−Q−[SiY3-x1 xzy (I)
{式中、Rf 1は、一官能性又は二官能性フッ素化基を表し、
Qは、独立して、有機二官能性又は三官能性結合基を表し、
1は、独立して、C1〜C4アルキル基を表し、
Yは、独立して、C1〜C4アルコキシ基、又は構造式−O−A−R3の親水性アルコキシ基を表すが、但し、少なくとも1つのYが前記親水性アルコキシ基であり、式中、各Aは、独立して、a)式、(CHR2−CH2O)q(式中、qは、1〜40の値を有する数であり、R2は、独立して水素又はメチルであり、R2の少なくとも70%は水素である)を有するか、又は(b)1つのOHおよび1つのヒドロキシル水素を除去することにより、ポリオール、又は、そのアルキルエーテル又はポリエーテル誘導体から誘導される、二官能性親水基を含み、
および、式中、R3は独立して、水素、又は炭素原子数1〜4の低級アルキル基であり、
xは、0又は1であり、
yは、1又は2であり、
zは、1又は2である}、および
(b)少なくとも1種類の水と完全に混和性の有機補助溶媒と少なくとも1種類のフッ素化界面活性剤のうちの一方又は両方、
を含む均一な混合物を含む、希釈可能な非水性濃縮物。
(A) at least one self-emulsifying fluorinated alkoxysilane of formula I,
R f 1 - [- Q- [ SiY 3-x R 1 x] z] y (I)
{Wherein R f 1 represents a monofunctional or difunctional fluorinated group;
Q independently represents an organic difunctional or trifunctional linking group;
R 1 independently represents a C 1 -C 4 alkyl group,
Y independently represents a C 1 to C 4 alkoxy group or a hydrophilic alkoxy group of the structural formula —O—A—R 3 , provided that at least one Y is the hydrophilic alkoxy group ; Wherein each A is independently a) a formula, (CHR 2 —CH 2 O) q , wherein q is a number having a value from 1 to 40 and R 2 is independently hydrogen or Or at least 70% of R 2 is hydrogen) or (b) derived from a polyol or its alkyl ether or polyether derivative by removing one OH and one hydroxyl hydrogen Containing a bifunctional hydrophilic group,
In the formula, R 3 is independently hydrogen or a lower alkyl group having 1 to 4 carbon atoms,
x is 0 or 1,
y is 1 or 2,
z is 1 or 2}, and (b) one or both of at least one water fully miscible organic co-solvent and at least one fluorinated surfactant,
A dilutable non-aqueous concentrate comprising a homogeneous mixture comprising
a.水、又は、水と少なくとも1種類の有機補助溶媒とを含む水性溶媒混合物を含む、希釈媒体、および
b.i.式Iの少なくとも1種類の自己乳化性フッ素化アルコキシシラン、
f 1−[−Q−[SiY3-x1 xzy (I)
{式中、Rf 1は、−(Cn2n)−、−(Cn2nO)−、−(CF(Z))−、−(CF(Z)O)−、−(CF(Z)Cn2nO)−、−(Cn2nCF(Z)O)−およびこれらの組合せからなる群から選択される過フッ素化繰り返し単位を含む、一官能性又は二官能性パーフルオロポリエーテルを表し、式中、Zは、フッ素原子、パーフルオロアルキル基、酸素置換パーフルオロアルキル基、パーフルオロアルコキシ基、および酸素置換パーフルオロアルコキシ基であり、そして、式中、nは1〜6であり、
Qは、独立して、有機二官能性又は三官能性結合基を表し、
1は、独立して、C1〜C4アルキル基を表し、
Yは、独立して、C1〜C4アルコキシ基、又は構造式−O−A−R3の親水性アルコキシ基を表すが、但し、少なくとも1つの親水性アルコキシ基がフッ素化アルコキシシラン中に存在し、式中、各Aは、独立して、a)式、(CHR2−CH2O)q(式中、qは、1〜40の値を有する数であり、R2は、独立して水素又はメチルであり、R2の少なくとも70%が水素である)を有するか、又は(b)1つのOHおよび1つのヒドロキシル水素を除去することにより、ポリオール、又は、そのアルキルエーテル又はポリエーテル誘導体から誘導される、二官能性親水基を含み、
および、式中、R3は独立して、水素、又は炭素原子数1〜4の低級アルキル基であり、
xは、0又は1であり、
yは、1又は2であり、
zは、1又は2である}、および
ii.少なくとも1種類の水に完全に混和性の有機補助溶媒と少なくとも1種類のフッ素化界面活性剤のうちの一方又は両方、
を含む、均一な混合物を含む希釈可能な非水性濃縮物、
を含む水性希釈液。
a. A dilution medium comprising water or an aqueous solvent mixture comprising water and at least one organic co-solvent; and b. i. At least one self-emulsifying fluorinated alkoxysilane of formula I;
R f 1 - [- Q- [ SiY 3-x R 1 x] z] y (I)
{Wherein, R f 1 is, - (C n F 2n) -, - (C n F 2n O) -, - (CF (Z)) -, - (CF (Z) O) -, - (CF (Z) C n F 2n O ) -, - (C n F 2n CF (Z) O) - is selected from the group consisting of including perfluorinated repeating units, monofunctional or difunctional Represents a perfluoropolyether, wherein Z is a fluorine atom, a perfluoroalkyl group, an oxygen-substituted perfluoroalkyl group, a perfluoroalkoxy group, and an oxygen-substituted perfluoroalkoxy group, and wherein n is 1-6,
Q independently represents an organic difunctional or trifunctional linking group;
R 1 independently represents a C 1 -C 4 alkyl group,
Y independently represents a C 1 to C 4 alkoxy group or a hydrophilic alkoxy group of the structural formula —O—A—R 3 , provided that at least one hydrophilic alkoxy group is present in the fluorinated alkoxysilane. Wherein each A is independently a) a formula, (CHR 2 —CH 2 O) q , where q is a number having a value of 1-40, and R 2 is independently Or at least 70% of R 2 is hydrogen) or (b) by removing one OH and one hydroxyl hydrogen, the polyol or its alkyl ether or poly Containing a bifunctional hydrophilic group derived from an ether derivative;
In the formula, R 3 is independently hydrogen or a lower alkyl group having 1 to 4 carbon atoms,
x is 0 or 1,
y is 1 or 2,
z is 1 or 2}, and ii. One or both of at least one water-miscible organic cosolvent and at least one fluorinated surfactant;
A dilutable non-aqueous concentrate comprising a homogeneous mixture,
An aqueous diluent containing
基材に請求項に記載の水性希釈液を塗布する工程、および前記水性希釈液を硬化させる工程を含む、基材の処理方法。 The processing method of a base material including the process of apply | coating the aqueous dilution liquid of Claim 2 to a base material, and the process of hardening | curing the said aqueous dilution liquid. a.基材、および
b.請求項に記載の水性希釈液を前記基材上に塗付し、前記水性希釈液を硬化させることにより得られる、前記基材上の塗膜、
を含む物品。
a. A substrate, and b. A coating film on the substrate obtained by applying the aqueous diluent according to claim 2 on the substrate and curing the aqueous diluent,
Articles containing.
前記基材がガラス、セラミック、又は、反射防止フィルムの少なくともいずれか1つを含む、請求項に記載の物品。 The article of claim 4 , wherein the substrate comprises at least one of glass , ceramic, or antireflective film .
JP2003547500A 2001-11-27 2002-10-25 Composition for water-based delivery of self-emulsifying fluorinated alkoxysilanes Pending JP2005510607A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/994,561 US20030113555A1 (en) 2001-11-27 2001-11-27 Compositions for aqueous delivery of self-emulsifying fluorinated alkoxysilanes
PCT/US2002/034280 WO2003046056A1 (en) 2001-11-27 2002-10-25 Compositions for aqueous delivery of self-emulsifying fluorinated alkoxysilanes

Publications (2)

Publication Number Publication Date
JP2005510607A JP2005510607A (en) 2005-04-21
JP2005510607A5 true JP2005510607A5 (en) 2006-01-05

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Country Status (7)

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US (1) US20030113555A1 (en)
EP (1) EP1448677A1 (en)
JP (1) JP2005510607A (en)
CN (1) CN1285645C (en)
AU (1) AU2002357671A1 (en)
MX (1) MXPA04004978A (en)
WO (1) WO2003046056A1 (en)

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US20040241396A1 (en) * 2003-05-29 2004-12-02 3M Innovative Properties Company Method of modifying a surface of a substrate and articles therefrom
US20040241323A1 (en) * 2003-05-29 2004-12-02 3M Innovative Properties Company Method for applying adhesive to a substrate
US20040241395A1 (en) * 2003-05-29 2004-12-02 3M Innovative Properties Company Method of modifying a surface of a substrate and articles therefrom
US6969166B2 (en) * 2003-05-29 2005-11-29 3M Innovative Properties Company Method for modifying the surface of a substrate
US7652115B2 (en) * 2003-09-08 2010-01-26 3M Innovative Properties Company Fluorinated polyether isocyanate derived silane compositions
US7141537B2 (en) * 2003-10-30 2006-11-28 3M Innovative Properties Company Mixture of fluorinated polyethers and use thereof as surfactant
US7803894B2 (en) * 2003-12-05 2010-09-28 3M Innovatie Properties Company Coating compositions with perfluoropolyetherisocyanate derived silane and alkoxysilanes
US7321018B2 (en) 2003-12-23 2008-01-22 3M Innovative Properties Company Compositions for aqueous delivery of fluorinated oligomeric silanes
EP1942225A4 (en) * 2005-09-21 2012-05-30 Daikin Ind Ltd Treatment for paper and method for treatment of paper
US7964552B2 (en) 2006-12-15 2011-06-21 E. I. Du Pont De Nemours And Company Fluorosurfactant with disproportionate effect
US20080146820A1 (en) * 2006-12-15 2008-06-19 Axel Hans-Joachim Herzog Phosphate fluorosurfactant and siloxane surfactant
CN105037412A (en) * 2007-10-01 2015-11-11 3M创新有限公司 Cationic fluorinated ether silane compositions and related methods
US8501641B2 (en) * 2007-10-01 2013-08-06 3M Innovative Properties Company Compositions comprising cationic fluorinated ether silanes, and related methods
JPWO2009069183A1 (en) * 2007-11-30 2011-04-07 小川 一文 Humidity control material
EP2412779A4 (en) * 2009-03-25 2014-01-15 Daikin Ind Ltd Surfactant comprising fluorine-containing polymer
WO2013106383A1 (en) 2012-01-10 2013-07-18 3M Innovative Properties Company Aqueous fluorinated silane dispersions
WO2014137801A1 (en) * 2013-03-03 2014-09-12 John Moore Temporary adhesive with tunable adhesion force sufficient for processing thin solid materials
KR20200021200A (en) * 2018-08-20 2020-02-28 삼성전자주식회사 Surface coating material and film and stacked structure and display device
CN115537120B (en) * 2022-11-03 2023-07-21 山东省科学院新材料研究所 Heat-resistant grafted silicone resin coating and preparation method thereof

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AU632869B2 (en) * 1989-12-14 1993-01-14 Minnesota Mining And Manufacturing Company Fluorocarbon-based coating compositions and articles derived therefrom
US5702509A (en) * 1995-12-22 1997-12-30 Minnesota Mining And Manufacturing Company Masonry treatment composition
US6277485B1 (en) * 1998-01-27 2001-08-21 3M Innovative Properties Company Antisoiling coatings for antireflective surfaces and methods of preparation
US6613860B1 (en) * 2000-10-12 2003-09-02 3M Innovative Properties Company Compositions comprising fluorinated polyether silanes for rendering substrates oil and water repellent

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